SIFM 2019 Poster Archive

“Targeting miRNAs as a novel therapy for STXBP1 epileptic encephalopathy”

CHoP / University of Pennsylvania Perelman School of Medicine

Development of human neuronal networks and preclinical mouse models to test novel therapies for STXBP1 haploinsufficiency

Columbia Precision Medicine

STXBP1 haploinsufficient mice recapitulate many features of STXBP1 encephalopathy

Texas Children’s Hospital / Baylor School of Medicine

An integrative approach to STXBP1-Encephalopathy: in vitro, in vivo and patient clinics

VU University of Amsterdam

Mechanism-Based Rescue of Munc18-1 Dysfunction in Varied Encephalopathies by Chemical Chaperones

Weill Cornell Medicine

MUNC18-1 / STXBP1 Instability in Infantile Epileptic Encephalpathies is Rescued by Pharmacological Chaperones”

Weill Cornell Medicine